Epinephrine Injection USP, 1 mL, USP 1:1000 (1 mg/mL), SQ/IM, Hospira, Inc., Lake Forest, IL --- NDC 0409-7241-01
Reported: January 9, 2013 Initiated: October 25, 2012 #D-106-2013
Product Description
Epinephrine Injection USP, 1 mL, USP 1:1000 (1 mg/mL), SQ/IM, Hospira, Inc., Lake Forest, IL --- NDC 0409-7241-01
Reason for Recall
Presence of Particulates; may contain glass particles
Details
- Recalling Firm
- Hospira Inc.
- Units Affected
- 361,600/1-mL ampules
- Distribution
- Nationwide
- Location
- Lake Forest, IL
Frequently Asked Questions
What product was recalled? ▼
Epinephrine Injection USP, 1 mL, USP 1:1000 (1 mg/mL), SQ/IM, Hospira, Inc., Lake Forest, IL --- NDC 0409-7241-01. Recalled by Hospira Inc.. Units affected: 361,600/1-mL ampules.
Why was this product recalled? ▼
Presence of Particulates; may contain glass particles
Which agency issued this recall? ▼
This recall was issued by the FDA Drug on January 9, 2013. Severity: Moderate. Recall number: D-106-2013.
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